process that is gone through in order for a device to receive approval by a government regulatory agency. This includes any required preclinical or clinical testing, review, submission, and evaluation of the applications and test results, and post-marketing surveillance. It is not restricted to fda.
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... Jeez., thanks man! IRB Review: Type of Review: Full Board Most Recent Approval: June 07, 1995 Number of Human Subjects in the Last Reporting Period ... liquid, or gas ) in human subjects. For diagnostic research. Instrument/Device/Product Testing or Man-Machine Studies: Use of human subjects to ...
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